CA2059088A1 - Pesticidal 1-(2-pyridyl)pyrazoles - Google Patents
Pesticidal 1-(2-pyridyl)pyrazolesInfo
- Publication number
- CA2059088A1 CA2059088A1 CA002059088A CA2059088A CA2059088A1 CA 2059088 A1 CA2059088 A1 CA 2059088A1 CA 002059088 A CA002059088 A CA 002059088A CA 2059088 A CA2059088 A CA 2059088A CA 2059088 A1 CA2059088 A1 CA 2059088A1
- Authority
- CA
- Canada
- Prior art keywords
- substituted
- halogen
- alkyl
- alkoxy
- moieties
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- XXTPHXNBKRVYJI-UHFFFAOYSA-N 2-pyrazol-1-ylpyridine Chemical class C1=CC=NN1C1=CC=CC=N1 XXTPHXNBKRVYJI-UHFFFAOYSA-N 0.000 title abstract 2
- 230000000361 pesticidal effect Effects 0.000 title abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 125000003545 alkoxy group Chemical group 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000002367 halogens Chemical group 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 238000006467 substitution reaction Methods 0.000 abstract 3
- 125000004647 alkyl sulfenyl group Chemical class 0.000 abstract 2
- 125000004644 alkyl sulfinyl group Chemical class 0.000 abstract 2
- 125000004390 alkyl sulfonyl group Chemical class 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 150000002431 hydrogen Chemical group 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 241000238876 Acari Species 0.000 abstract 1
- 241001124076 Aphididae Species 0.000 abstract 1
- 241000238421 Arthropoda Species 0.000 abstract 1
- 241000238631 Hexapoda Species 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 241000244206 Nematoda Species 0.000 abstract 1
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 abstract 1
- 125000004949 alkyl amino carbonyl amino group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 125000005221 halo alkyl carbonyl amino group Chemical group 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 244000000013 helminth Species 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Novel 1-(2-pyridyl)pyrazoles of formula (I) (see formula I) wherein:
X is a halogen, nitro or unsubstituted or halo-substituted alkylsulfenyl, alkylsulfinyl or alkylsulfonyl, wherein the alkyl moiety is a linear or branched chain, containing one to four carbon atoms, and where substituted, is substituted by one of more halogen atoms, which are the same or different, up to full substitution of the alkyl moiety;
Y is hydrogen, halogen, cyano, alkylsulfenyl, alkylsulfinyl, alkylsulfonyl, alkoxy, amino, alkylamino, dialkylamino, trialkylammanium salt, cyanoalkylamino, alkoxyalkylamino, alkoxycarbonylamino, alkylcarbonylamino, haloalkylcarbonylamino, alkylaminocarbonylamino, dialkylaminocarbonylamino or alkoxyalkylideneimino, wherein the alkyl and alkoxy moieties are linear or branched and contain one to four carbon atoms, and the haloalkyl moieties are substituted by one or more halogen atoms, which are the same or different, up to full substitution of the alkyl moiety;
Z is cyano or halogen; and R2, R3, R4 and R5 are each individually hydrogen, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, cyano or vitro, wherein the alkyl and alkoxy moieties are linear or branched and contain one to four carbon atoms, and the halo-substituted moieties are substituted by one or more halogen atoms, which are the same or different, up to full substitution of the alkyl and alkoxy moieties; at least one of R2 to R5 being other then hydrogen.
The invention further relates to intermediates and processes to make the compounds, pesticidal compositions comprising the compounds, and methods of use of the compounds for the control of arthropods (mites, aphids or insects) nematodes, helminths or protozoa.
X is a halogen, nitro or unsubstituted or halo-substituted alkylsulfenyl, alkylsulfinyl or alkylsulfonyl, wherein the alkyl moiety is a linear or branched chain, containing one to four carbon atoms, and where substituted, is substituted by one of more halogen atoms, which are the same or different, up to full substitution of the alkyl moiety;
Y is hydrogen, halogen, cyano, alkylsulfenyl, alkylsulfinyl, alkylsulfonyl, alkoxy, amino, alkylamino, dialkylamino, trialkylammanium salt, cyanoalkylamino, alkoxyalkylamino, alkoxycarbonylamino, alkylcarbonylamino, haloalkylcarbonylamino, alkylaminocarbonylamino, dialkylaminocarbonylamino or alkoxyalkylideneimino, wherein the alkyl and alkoxy moieties are linear or branched and contain one to four carbon atoms, and the haloalkyl moieties are substituted by one or more halogen atoms, which are the same or different, up to full substitution of the alkyl moiety;
Z is cyano or halogen; and R2, R3, R4 and R5 are each individually hydrogen, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, cyano or vitro, wherein the alkyl and alkoxy moieties are linear or branched and contain one to four carbon atoms, and the halo-substituted moieties are substituted by one or more halogen atoms, which are the same or different, up to full substitution of the alkyl and alkoxy moieties; at least one of R2 to R5 being other then hydrogen.
The invention further relates to intermediates and processes to make the compounds, pesticidal compositions comprising the compounds, and methods of use of the compounds for the control of arthropods (mites, aphids or insects) nematodes, helminths or protozoa.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US64353091A | 1991-01-18 | 1991-01-18 | |
US643,530 | 1991-01-18 |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2059088A1 true CA2059088A1 (en) | 1992-07-19 |
CA2059088C CA2059088C (en) | 2002-06-18 |
Family
ID=24581208
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002059088A Expired - Lifetime CA2059088C (en) | 1991-01-18 | 1992-01-09 | Pesticidal 1-(2-pyridyl)pyrazoles |
Country Status (32)
Country | Link |
---|---|
US (1) | US5306694A (en) |
EP (1) | EP0500209B1 (en) |
JP (1) | JP3140829B2 (en) |
KR (1) | KR100225658B1 (en) |
CN (2) | CN1041269C (en) |
AT (1) | ATE158290T1 (en) |
AU (1) | AU644259B2 (en) |
BG (1) | BG61813B1 (en) |
BR (1) | BR9200219A (en) |
CA (1) | CA2059088C (en) |
CZ (1) | CZ281976B6 (en) |
DE (1) | DE69222202T2 (en) |
DK (1) | DK0500209T3 (en) |
EG (1) | EG19658A (en) |
ES (1) | ES2106821T3 (en) |
FI (1) | FI105028B (en) |
GR (1) | GR3025572T3 (en) |
HU (1) | HU208534B (en) |
IE (1) | IE920146A1 (en) |
IL (1) | IL100678A (en) |
MA (1) | MA22390A1 (en) |
MX (1) | MX9200182A (en) |
MY (1) | MY108659A (en) |
NO (1) | NO179282C (en) |
NZ (1) | NZ241314A (en) |
OA (1) | OA09756A (en) |
PL (1) | PL168730B1 (en) |
RO (1) | RO109940B1 (en) |
RU (1) | RU2088580C1 (en) |
TR (1) | TR25675A (en) |
UY (1) | UY23358A1 (en) |
ZW (1) | ZW1192A1 (en) |
Families Citing this family (90)
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JPH02142785A (en) * | 1988-11-22 | 1990-05-31 | Mitsubishi Petrochem Co Ltd | 5-amino-4-chloro-1-pyridylpyrazole derivative |
US4918085A (en) * | 1989-03-02 | 1990-04-17 | Rhone-Poulenc Ag Company | Pesticidal 3-cyano-5-alkoxy-1-arylpyrazoles, compositions and use |
PH27357A (en) * | 1989-09-22 | 1993-06-21 | Fujisawa Pharmaceutical Co | Pyrazole derivatives and pharmaceutical compositions comprising the same |
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1992
- 1992-01-08 NO NO920097A patent/NO179282C/en not_active IP Right Cessation
- 1992-01-09 CA CA002059088A patent/CA2059088C/en not_active Expired - Lifetime
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- 1992-01-15 AU AU10251/92A patent/AU644259B2/en not_active Expired
- 1992-01-16 EG EG3092A patent/EG19658A/en active
- 1992-01-16 MY MYPI92000074A patent/MY108659A/en unknown
- 1992-01-16 ZW ZW11/92A patent/ZW1192A1/en unknown
- 1992-01-16 CZ CS92130A patent/CZ281976B6/en not_active IP Right Cessation
- 1992-01-16 IL IL10067892A patent/IL100678A/en not_active IP Right Cessation
- 1992-01-16 MX MX9200182A patent/MX9200182A/en unknown
- 1992-01-16 BR BR929200219A patent/BR9200219A/en not_active IP Right Cessation
- 1992-01-17 RU SU925010813A patent/RU2088580C1/en active
- 1992-01-17 IE IE014692A patent/IE920146A1/en unknown
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- 1992-01-17 FI FI920221A patent/FI105028B/en active
- 1992-01-17 OA OA60130A patent/OA09756A/en unknown
- 1992-01-17 TR TR92/0075A patent/TR25675A/en unknown
- 1992-01-17 HU HU9200170A patent/HU208534B/en unknown
- 1992-01-17 BG BG95776A patent/BG61813B1/en unknown
- 1992-01-17 RO RO149204A patent/RO109940B1/en unknown
- 1992-01-17 JP JP04044353A patent/JP3140829B2/en not_active Expired - Lifetime
- 1992-01-18 KR KR1019920000700A patent/KR100225658B1/en not_active IP Right Cessation
- 1992-01-18 CN CN92100330A patent/CN1041269C/en not_active Expired - Lifetime
- 1992-01-20 DE DE69222202T patent/DE69222202T2/en not_active Expired - Lifetime
- 1992-01-20 DK DK92300467.5T patent/DK0500209T3/en active
- 1992-01-20 ES ES92300467T patent/ES2106821T3/en not_active Expired - Lifetime
- 1992-01-20 UY UY23358A patent/UY23358A1/en unknown
- 1992-01-20 AT AT92300467T patent/ATE158290T1/en not_active IP Right Cessation
- 1992-01-20 EP EP92300467A patent/EP0500209B1/en not_active Expired - Lifetime
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1993
- 1993-06-17 US US08/079,221 patent/US5306694A/en not_active Expired - Lifetime
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1997
- 1997-12-02 GR GR970403222T patent/GR3025572T3/en unknown
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1998
- 1998-04-08 CN CN98106376A patent/CN1103771C/en not_active Expired - Lifetime
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